Canonical Allele Identifier: CA2022897966
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245195T= , CM000674.2:g.25245195T= GRCh38
NC_000012.11:g.25398129T= , CM000674.1:g.25398129T= GRCh37
NC_000012.10:g.25289396T= NCBI36
NG_007524.1:g.10726A=
NG_007524.2:g.10809A=

Transcript Alleles

HGVS Amino-acid change
ENST00000556131.2:c.111+79A= ENSP00000451856.1:n.111+79A=
ENST00000557334.6:c.111+79A= ENSP00000452512.1:n.111+79A=
ENST00000685328.1:c.111+79A= ENSP00000508921.1:n.111+79A=
ENST00000686877.1:c.111+79A= ENSP00000510431.1:n.111+79A=
ENST00000686969.1:c.111+79A= ENSP00000510479.1:n.111+79A=
ENST00000687356.1:c.111+79A= ENSP00000510511.1:n.111+79A=
ENST00000688940.1:c.111+79A= ENSP00000509238.1:n.111+79A=
ENST00000690804.1:c.111+79A= ENSP00000508568.1:n.111+79A=
ENST00000692768.1:c.-88+5556A= ENSP00000510254.1:n.-88+5556A=
ENST00000693229.1:c.111+79A= ENSP00000509223.1:n.111+79A=
ENST00000256078.10:c.111+79A= MANE Plus Clinical ENSP00000256078.5:n.111+79A=
ENST00000311936.8:c.111+79A= MANE Select ENSP00000308495.3:n.111+79A=
ENST00000256078.8:c.111+79A= ENSP00000256078.4:n.111+79A=
ENST00000311936.7:c.111+79A= ENSP00000308495.3:n.111+79A=
ENST00000556131.1:c.111+79A= ENSP00000451856.1:n.111+79A=
ENST00000557334.5:c.111+79A= ENSP00000452512.1:n.111+79A=
NM_004985.4:c.111+79A= NP_004976.2:n.111+79A=
NM_033360.3:c.111+79A= NP_203524.1:n.111+79A=
XM_006719069.2:c.111+79A= XP_006719132.1:n.111+79A=
XM_011520653.1:c.111+79A= XP_011518955.1:n.111+79A=
XM_006719069.4:c.111+79A= XP_006719132.1:n.111+79A=
XM_011520653.3:c.111+79A= XP_011518955.1:n.111+79A=
NM_001369786.1:c.111+79A= NP_001356715.1:n.111+79A=
NM_001369787.1:c.111+79A= NP_001356716.1:n.111+79A=
NM_004985.5:c.111+79A= MANE Select NP_004976.2:n.111+79A=
NM_033360.4:c.111+79A= MANE Plus Clinical NP_203524.1:n.111+79A=